Overview of 3Rs opportunities in drug discovery and development using non-human primates

Q3 Pharmacology, Toxicology and Pharmaceutics
Helen Prior , Fiona Sewell , Jane Stewart
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引用次数: 10

Abstract

Non-human primates (NHPs) are included within safety testing programmes for potential new medicines when justified as the relevant species for use. Although the NHP is often the only relevant species for the testing of large molecule biotherapeutics, a proportion of small molecule compounds may also require testing in NHPs, when other non-rodent species are unsuitable. Whilst the toxicology studies continue to be required for regulatory submissions, there are opportunities to both reduce the number of animals and refine procedures used within the studies, by implementation of best practice study designs and processes identified by NC3Rs-industry data sharing projects. With the rapid expansion of biotherapeutics within the industry expected to continue or increase, the number of compounds within company pipelines, and hence the number of NHPs used for testing, are likewise anticipated to grow. A wider acceptance and adoption of established 3Rs approaches should continue to minimise the use of NHPs whilst maximising the potential these new therapies bring to improve human health.

利用非人类灵长类动物进行药物发现和开发的3Rs机会概述
非人灵长类动物(NHPs)在有理由作为相关物种使用时被纳入潜在新药的安全性测试规划。虽然NHP通常是大分子生物治疗药物测试的唯一相关物种,但当其他非啮齿动物物种不适合时,也可能需要在NHP中测试一小部分小分子化合物。虽然毒理学研究仍然需要提交监管报告,但通过实施nc3rs -行业数据共享项目确定的最佳实践研究设计和过程,有机会减少动物数量并改进研究中使用的程序。随着行业内生物疗法的快速扩张预计将继续或增加,公司管道内的化合物数量以及用于测试的nhp数量也预计会增加。更广泛地接受和采用既定的3Rs方法应继续尽量减少NHPs的使用,同时最大限度地发挥这些新疗法改善人类健康的潜力。
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来源期刊
Drug Discovery Today: Disease Models
Drug Discovery Today: Disease Models Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
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期刊介绍: Drug Discovery Today: Disease Models discusses the non-human experimental models through which inference is drawn regarding the molecular aetiology and pathogenesis of human disease. It provides critical analysis and evaluation of which models can genuinely inform the research community about the direct process of human disease, those which may have value in basic toxicology, and those which are simply designed for effective expression and raw characterisation.
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